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Venous Compression in Fontan

Venous Function and the Effect of Venous Compression on Exercise Cardiovascular Function in Patients With Fontan Circulation.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07220226
Enrollment
20
Registered
2025-10-23
Start date
2026-05-10
Completion date
2027-11-01
Last updated
2026-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fontan Circulation, Single-ventricle

Keywords

Venous Compression, Exercise Testing, Cardiac Reserve, Fontan Circulation, Magnetic Resonance Imaging, vascular function

Brief summary

The aim of this study is to investigate whether venous compression garments increase exercise stroke volume in patients with Fontan circulation. To address this aim, we will test the following hypotheses: 1. Acute and chronic external venous compression will increase exercise stroke volume in patients with Fontan circulation. 2. Patients with significant venous varicosities will have a greater response to venous compression. Participants will: * Undergo submaximal exercise testing in MRI to measure venous return and exercise stroke volume with and without the wearing of compression garments * Undergo submaximal exercise testing on a seated upright exercise ergometer with concurrent measurement of stroke volume with and without the wearing of compression garments * A subset of participants will repeat both testing visits after wearing compression garments for 2-weeks during waking hours. Participants will: * Undergo submaximal exercise testing in MRI to measure venous return and exercise stroke volume with and without the wearing of compression garments * Undergo submaximal exercise testing on a seated upright exercise ergometer with concurrent measurement of stroke volume with and without the wearing of compression garments * A subset of participants will repeat both testing visits after wearing compression garments for 2-weeks during waking hours.

Detailed description

Study Day 1 - Consent, Screening and Garment Measurements: Following assessment of participant eligibility, all participants will undergo leg venous ultrasound assessment and abdominal-foot measurements for the custom making of compression garments. Study Day 2 - MRI: Study participants will undergo comprehensive cardiovascular MRI using a 3T MRI scanner with and without compression garments and exercise. Study Day 3 - Cardiovascular & Exercise Testing Day: All participants will undergo comprehensive cardiovascular structure and function assessments at rest and during exercise with and without the wearing of compression garments. Baseline testing will include dual x-ray absorptiometry (DEXA), pulmonary function testing, comprensive vascular assessments and echocardiography. During exercise at two submaximal workloads, the study team will measure blood pressure, oxygen uptake and cardiac output.

Interventions

Acute and 2-week effects of compression garments

OTHERWithout compression garments

Acute effects without compression garments

Sponsors

University of Texas Southwestern Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

Patients with a Fontan circulation - Inclusion criteria: • Patients at UTSW aged 18-45 years old with a Fontan circulation.

Exclusion criteria

* NYHA Class 4 * Severe AV valve regurgitation * Severe ventricular dysfunction * Large ascites * Significant varicosities * Atrio-pulmonary (AP) Fontan * Known Fontan thrombus * Poorly controlled arrythmia * Unplanned cardiac admission in the last 6 months * Cyanosis (resting O2 saturation \<85%) * Pregnant * Common femoral vein obstruction \>50% to be performed following completion of informed consent. Healthy Controls: Healthy control participants will be recruited on the basis of having no known chronic diseases and not currently taking any cardiovascular medications.

Design outcomes

Primary

MeasureTime frameDescription
Change in Stroke Volume with ExerciseRest (20 minutes), Exercise (10 minutes)The change in single ventricular stroke volume from rest to moderate intensity exercise with compression garments during baseline testing
The Acute Effect of Compression Garments on Stroke Volume during ExerciseRest (20 minutes) and Exercise (10 minutes) repeated during baseline testingThe difference in the change in single ventricular stroke volume during moderate intensity exercise between baseline testing with (outcome #1) and without (outcome #2) garments
The Chronic Effect of Compression Garments on Stroke Volume during exerciseRest (20 minutes) and Exercise (10 minutes) completed during baseline and during follow-up testingThe difference in the change in single ventricular stroke volume during moderate intensity exercise between baseline testing without garments (outcome #2) and following 2 weeks of wearing compression garments (outcome #3) in patients with Fontan Circulation.

Secondary

MeasureTime frameDescription
Change in Venous Return with ExerciseRest (10 minutes) and Exercise (5 minutes)The change in inferior vena cava flow from rest to moderate intensity exercise with compression garments using MRI during baseline testing
The Acute Effect of Compression Garments on Changes in Venous Return with ExerciseRest (10 minutes) and Exercise (5 minutes) repeated during baseline testingThe difference in the change in inferior vena cava flow during moderate intensity exercise between baseline testing with (outcome #6) and without (outcome #7) garments
The Chronic Effect of Compression Garments on Changes in Venous Return with ExerciseRest (10 minutes) and Exercise (5 minutes) completed during baseline and during follow-up testingThe difference in the change in inferior vena cava flow during moderate intensity exercise between baseline testing without garments (outcome #7) and following 2 weeks of wearing compression garments (outcome #8) in patients with Fontan Circulation.

Countries

United States

Contacts

CONTACTKeri Shafer, MD
keri.shafer@utsouthwestern.edu2146451165
CONTACTDenis J Wakeham, PhD
denis.wakeham@utsouthwestern.edu2146451165
PRINCIPAL_INVESTIGATORKeri Shafer, MD

University of Texas Southwestern Medical Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 31, 2026